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Merck

45674

Sigma-Aldrich

Erythromycin

tested according to Ph. Eur.

Synonim(y):

Erythromycinum

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About This Item

Wzór empiryczny (zapis Hilla):
C37H67NO13
Numer CAS:
Masa cząsteczkowa:
733.93
Beilstein:
75279
Numer WE:
Numer MDL:
Kod UNSPSC:
51282304
Identyfikator substancji w PubChem:
NACRES:
NA.76

agency

EPA 1694
USP/NF
tested according to Ph. Eur.

Poziom jakości

Postać

solid

kolor

white to faint yellow

rozpuszczalność

H2O: soluble 2 mg/mL
acetone: freely soluble
acetonitrile: freely soluble
alcohol: soluble
amyl acetate: moderately soluble
chloroform: soluble
diethyl ether: soluble
ethyl acetate: freely soluble

spektrum działania antybiotyku

Gram-negative bacteria
Gram-positive bacteria

Zastosowanie

environmental

Tryb działania

protein synthesis | interferes

ciąg SMILES

CC[C@H]1OC(=O)[C@H](C)[C@@H](O[C@H]2C[C@@](C)(OC)[C@@H](O)[C@H](C)O2)[C@H](C)[C@@H](O[C@@H]3O[C@H](C)C[C@@H]([C@H]3O)N(C)C)[C@](C)(O)C[C@@H](C)C(=O)[C@H](C)[C@@H](O)[C@]1(C)O

InChI

1S/C37H67NO13/c1-14-25-37(10,45)30(41)20(4)27(39)18(2)16-35(8,44)32(51-34-28(40)24(38(11)12)15-19(3)47-34)21(5)29(22(6)33(43)49-25)50-26-17-36(9,46-13)31(42)23(7)48-26/h18-26,28-32,34,40-42,44-45H,14-17H2,1-13H3/t18-,19-,20+,21+,22-,23+,24+,25-,26+,28-,29+,30-,31+,32-,34+,35-,36-,37-/m1/s1

Klucz InChI

ULGZDMOVFRHVEP-RWJQBGPGSA-N

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Opis ogólny

Chemical structure: macrolide

Zastosowanie

Erythromycin is an antibiotic produced by growth of certain strains of Streptomyces erythreus. This product is composed largely of erythromycin A with small amounts of erythromycins B and C and is recommended for concentration at 100 mg/L. Concentrations between 50 and 200 mg/L have also proven effective in controlling bacterial growth. Erythromycin has been used as a motilin receptor agonist, to block respiratory glycoconjugate secretion in human airways in vitro††, and for selecting plasmid-cured and recombinant lactococcus lactis MG1363 strains.

Działania biochem./fizjol.

Mode of Action: Erythromycin acts by inhibiting elongation at the transpeptidation step, specifically aminoacyl translocation from the A-site to P-site by binding to the 50s subunit of the bacterial 70s rRNA complex.

Antimicrobial Spectrum: This product acts against both gram-negative and gram-positive bacteria.

Opakowanie

25g

Przestroga

This product is stable in solution at 37°C for 3 days. Stock solutions should be stored at 2-8°C.

Uwaga dotycząca przygotowania

This product is soluble in water at 2 mg/mL, with a 0.067% solution in water yielding a pH of 8.0-10.5. It is also soluble in ethanol at 50 mg/mL, yielding a clear, colorless to faint yellow solution. It is freely soluble in alcohol, acetone, chloroform, acetonitrile and ethyl acetate but forms salts with acids. All solutions should be protected from light.

Inne uwagi

Keep container tightly closed in a dry and well-ventilated place.
This page may contain text that has been machine translated.

Kod klasy składowania

11 - Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves, type N95 (US)


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T Peeters et al.
The American journal of physiology, 257(3 Pt 1), G470-G474 (1989-09-01)
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Antibiotics targeting bacterial ribosomes disrupt protein synthesis, a key process in bacterial growth inhibition.

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